Evidence map›Paper›PMID 41057535›Full record

ArticleBritish journal of cancer2025

Serum multiomics prediction of prognosis and adverse reactions to concurrent chemoradiotherapy in patients with esophageal cancer.

Wen-Zhi Wu, He-Cheng Huang, Guang-Hui Zhu, Lian-Di Liao, Xu-Li Chen, Zhi-Mao Li, Man-Yu Chu, Shuai-Xia Yu, Dian Wang, En-Min Li and 1 more

Abstract read
In one paragraph

Article in British journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Wen-Zhi Wu *Chaoshan Branch of State Key Laboratory for Esophageal Cancer Prevention and Treatment, Department of Clinical Laboratory Medicine, Cancer Hospital, Shantou University Medical College, Shantou, 515041, Guangdong, China.
He-Cheng Huang *Shantou Central Hospital, Shantou, 515041, Guangdong, China.
Guang-Hui Zhu *Department of Forensic Medicine, Shantou University Medical College, Shantou, 515041, Guangdong, China.
Lian-Di LiaoThe Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Institute of Oncologic Pathology, Department of Pathology, Second Affiliated Hospital, Shantou University Medical College, Shantou, 515041, Guangdong, China.
Xu-Li ChenShantou Central Hospital, Shantou, 515041, Guangdong, China.
Zhi-Mao LiShantou Central Hospital, Shantou, 515041, Guangdong, China.
Man-Yu ChuThe Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Institute of Oncologic Pathology, Department of Pathology, Second Affiliated Hospital, Shantou University Medical College, Shantou, 515041, Guangdong, China.
Shuai-Xia YuThe Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Institute of Oncologic Pathology, Department of Pathology, Second Affiliated Hospital, Shantou University Medical College, Shantou, 515041, Guangdong, China.
Dian WangDepartment of Forensic Medicine, Shantou University Medical College, Shantou, 515041, Guangdong, China.
En-Min LiChaoshan Branch of State Key Laboratory for Esophageal Cancer Prevention and Treatment, Department of Clinical Laboratory Medicine, Cancer Hospital, Shantou University Medical College, Shantou, 515041, Guangdong, China. nmli@stu.edu.cn.ORCID http://orcid.org/0000-0001-6375-3614
Li-Yan XuChaoshan Branch of State Key Laboratory for Esophageal Cancer Prevention and Treatment, Department of Clinical Laboratory Medicine, Cancer Hospital, Shantou University Medical College, Shantou, 515041, Guangdong, China. lyxu@stu.edu.cn.ORCID http://orcid.org/0000-0002-1618-4292

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82173034
6 · The paper itself

Abstract

objectiveConcurrent chemoradiotherapy (CCRT) is an important treatment for patients with locally advanced esophageal squamous cell carcinoma (ESCC). There is still a lack of reliable means to predict efficacy, prognosis and hematologic toxicity.

designWe analyzed 127 serum samples before CCRT and 93 serum samples after CCRT from 127 ESCC patients via metabolomics by GC-MS. Combined with Olink proteomics, we constructed models to predict response and survival through machine learning. Multiple linear regression was used to construct hematologic toxicity prediction models. In combination with the proteomics of ESCC, metabolic changes were studied.

resultsA prediction model for the efficacy to CCRT was established via serum metabolomics and proteomics (Train, CR/nCR = 28/50, AUC = 0.9848, 95% CI = 0.9639-1.0000; Test, CR/nCR = 17/15, AUC = 0.8854, 95% CI = 0.7800-0.9908). A survival prediction model was established (n = 109, C-index = 0.7640, 95% CI = 0.7140-0.8140). Linear models for predicting hematologic toxicity were constructed (n = 111, R > 0.7). L-serine is important for the prognosis of patients with ESCC treated with CCRT, and SHMT2 is a key protein in serine metabolism that affects the efficacy of CCRT.

conclusionThe combination of serum metabolomics with proteomics can effectively predict the prognosis and hematologic toxicity, which can provide important data for patients to choose treatment methods.

Indexed as

ChemoradiotherapyEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaAdultAgedBiomarkers, TumorFemaleHumansMaleMetabolomicsMiddle AgedMultiomicsPrognosisProteomicsBiomarkers, Tumor

Identifiers

PMID41057535
PMCPMC12689725

What Socratic holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.